Canonical Allele Identifier: CA2581181694

Gene: POMT2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77279033G>C , CM000676.2:g.77279033G>C	GRCh38
NC_000014.8:g.77745376G>C , CM000676.1:g.77745376G>C	GRCh37
NC_000014.7:g.76815129G>C	NCBI36
NG_008897.1:g.46850C>G , LRG_844:g.46850C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555134.2:n.817-164C>G
ENST00000556394.2:c.1433-164C>G	ENSP00000451967.2:n.1433-164C>G
ENST00000682128.1:c.193-164C>G	ENSP00000506976.1:n.193-164C>G
ENST00000682247.1:c.1892-175C>G	ENSP00000507213.1:n.1892-175C>G
ENST00000682395.1:n.2356-164C>G
ENST00000682459.1:n.1595-164C>G
ENST00000682467.1:c.1892-525C>G	ENSP00000508062.1:n.1892-525C>G
ENST00000682615.1:n.246-164C>G
ENST00000682795.1:c.2039-164C>G	ENSP00000507574.1:n.2039-164C>G
ENST00000682895.1:n.1608-164C>G
ENST00000682955.1:n.1466-164C>G
ENST00000683095.1:c.298-164C>G	ENSP00000508040.1:n.298-164C>G
ENST00000683188.1:c.2153-164C>G
ENST00000683380.1:n.1556-164C>G
ENST00000683828.1:c.1601-164C>G
ENST00000683907.1:c.157-164C>G	ENSP00000507754.1:n.157-164C>G
ENST00000684172.1:c.268-164C>G	ENSP00000508391.1:n.268-164C>G
ENST00000684259.1:n.3495C>G
ENST00000684538.1:n.1107C>G
ENST00000684549.1:n.1443-164C>G
ENST00000261534.9:c.1892-164C>G MANE Select	ENSP00000261534.4:n.1892-164C>G
ENST00000261534.8:c.1892-164C>G	ENSP00000261534.4:n.1892-164C>G
ENST00000452340.7:n.2704C>G
ENST00000554767.5:n.2678-164C>G
ENST00000555134.1:n.817-164C>G
ENST00000555710.1:c.161-72C>G	ENSP00000451730.1:n.161-72C>G
ENST00000556171.1:c.484-164C>G
ENST00000556394.1:c.88-525C>G
ENST00000556446.1:n.29C>G
ENST00000602717.5:c.107-164C>G	ENSP00000487704.1:n.107-164C>G
NM_013382.5:c.1892-164C>G , LRG_844t1:c.1892-164C>G	NP_037514.2:n.1892-164C>G
XM_011536675.1:c.2081-164C>G	XP_011534977.1:n.2081-164C>G
XM_011536676.1:c.1748-164C>G	XP_011534978.1:n.1748-164C>G
XM_011536677.1:c.1622-164C>G	XP_011534979.1:n.1622-164C>G
XM_011536678.1:c.*465C>G	XP_011534980.1:n.*465C>G
XM_011536679.1:c.1175-164C>G	XP_011534981.1:n.1175-164C>G
XR_943416.1:n.2145-164C>G
XM_011536675.2:c.2081-164C>G	XP_011534977.1:n.2081-164C>G
XM_011536676.2:c.1748-164C>G	XP_011534978.1:n.1748-164C>G
XM_011536677.3:c.1622-164C>G	XP_011534979.1:n.1622-164C>G
XR_001750279.1:n.2178-164C>G
XR_001750282.1:n.2831-164C>G
XR_943416.3:n.2143-164C>G
NM_013382.6:c.1892-164C>G	NP_037514.2:n.1892-164C>G
NM_013382.7:c.1892-164C>G MANE Select	NP_037514.2:n.1892-164C>G